A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv558782



Internal ID16346191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:45861212..45892900hg38UCSC Ensembl
Innerchr12:46254995..46286683hg19UCSC Ensembl
Innerchr12:44541262..44572950hg18UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3831689
hg1931689
hg1831689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv795290
Samples
Known GenesARID2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv558782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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